The following data is part of a premarket notification filed by Siemens Hearing Instruments, Inc. with the FDA for Siemens Model 283 Asp.
| Device ID | K893575 |
| 510k Number | K893575 |
| Device Name: | SIEMENS MODEL 283 ASP |
| Classification | Hearing Aid, Air Conduction |
| Applicant | SIEMENS HEARING INSTRUMENTS, INC. 10 CORPORATE PLACE SOUTH CORPORATE PARK 287 Piscataway, NJ 08854 |
| Contact | Pamela Branderbit |
| Correspondent | Pamela Branderbit SIEMENS HEARING INSTRUMENTS, INC. 10 CORPORATE PLACE SOUTH CORPORATE PARK 287 Piscataway, NJ 08854 |
| Product Code | ESD |
| CFR Regulation Number | 874.3300 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1989-05-09 |
| Decision Date | 1990-05-21 |